Method of re-sensitizing vancomycin resistant bacteria which selectively cleave a cell wall depsipeptide

Inactive Publication Date: 2005-10-11
THE TRUSTEES OF COLUMBIA UNIV IN THE CITY OF NEW YORK +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

[0014]In addition, the present invention also provides a method of killing glycopeptide antibiotic resistant Gram-positive bacteria which comprises contacting the bacteria with an agent that selectively c

Problems solved by technology

One of the most challenging situations for the immuno-compromised patients is the development of vancomycin-re

Method used

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  • Method of re-sensitizing vancomycin resistant bacteria which selectively cleave a cell wall depsipeptide
  • Method of re-sensitizing vancomycin resistant bacteria which selectively cleave a cell wall depsipeptide
  • Method of re-sensitizing vancomycin resistant bacteria which selectively cleave a cell wall depsipeptide

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Embodiment Construction

[0032]This invention provides a method of treating a subject afflicted with an infection caused by glycopeptide antibiotic resistant Gram-positive bacteria, such as vancomycin resistant Gram-positive bacteria, in which resistance results from the conversion of an amide bond to an ester bond in the cell wall peptide precursors of the bacteria which comprises administering to the subject an antibacterial amount of vancomycin or a homolog of vancomycin and an amount of an agent effective to selectively cleave the ester bond so as to thereby treat the subject.

[0033]In one embodiment of the invention, the subject is a human being.

[0034]In general, the agent is an activated nucleophile and is further characterized by the presence within the agent of an electrophile and chirality complementary to a bacterial cell wall depsipeptide.

[0035]In one embodiment of the invention, the agent is represented by the formula S-Pro-Cn.

[0036]In another embodiment of the invention, the agent has the struct...

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Abstract

The present invention relates to pyrrolidine compounds of the general structure:
where n is an integer 1-6 and R is hydrogen or a C1 to C6 straight chain or branched alkyl group, and wherein when n=1, R=CH3 or H, useful for re-sensitizing vancomycin resistant Gram-positive bacteria in which resistance results from the conversion of an amide bond to an ester bond on the cell wall peptide precursors of the bacteria.

Description

[0001]This application is a continuation of U.S. Ser. No. 09 / 938,746, filed Aug. 23, 2001, now U.S. Pat. No. 6,734,165 now allowed, the contents of which are hereby incorporated by reference into the present application.[0002]The invention disclosed herein was made with Government support under NIH Grant No. 5-R01-HL-25634-18 from the National Institutes of Health. Accordingly, the U.S. Government has certain rights in this invention.[0003]Throughout this application, various references are identified by citations or a number in parenthesis, in which case their full citations appear on the pages following the Detailed Description immediately preceding the claims. Disclosure of these references in their entireties are hereby incorporated by reference into this application to more fully describe the state of the art to which this invention pertains.FIELD OF THE INVENTION[0004]The present invention relates to a method for re-sensitizing vancomycin resistant Gram-positive bacteria in wh...

Claims

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Application Information

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IPC IPC(8): A61K38/14A61K31/40
CPCA61K31/40A61K38/14A61K2300/00
Inventor CHIOSIS, GABRIELABONECA, IVO G.STILL, W. CLARK
Owner THE TRUSTEES OF COLUMBIA UNIV IN THE CITY OF NEW YORK
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